| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02024 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:110434970-110436090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:110435592-110435613 | CTCCTCCTCCTCCTCTCCTCC | - | 6.25 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_00603 | chr1:110434140-110436472 | Adipose_Nuclei | | SE_04393 | chr1:110434145-110435269 | Brain_Anterior_Caudate | | SE_06043 | chr1:110433946-110435699 | Brain_Hippocampus_Middle | | SE_53713 | chr1:110434526-110436227 | Spleen | | SE_62091 | chr1:110406355-110450750 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I109891 | chr1 | 110434463 | 110436093 |
|
Enhancer Sequence | CCTGCCCGGG CTAGAGATTG GACCCCAGCA TGGTTTTGGA GGCTGTAGAT TCAGCAGTTG 60
TGGTGTCACG AGTCACTCAT CTCAAATAAA GGACAGGGGG AACTCAGTGT GAGCCCCAAA 120
CAAGAAGCTC ACAGGCAGCT TCTGAGCCCT GGGGAGAAAT TGTTTGCTCC TGGGCTGGGT 180
GGTAAGGGGG GGTTCTCCAG TGGACCCTCC TTCCTCCACC TACTTGCCAC CAATTTGTAT 240
TGGGGAGGGG TTGGTATGCA GAGGGTGAAG ACAGTATCAT AAAAGCAGGA AAGTGTCCTG 300
AATTCCAGGG CTGAGGAAAC TCCCCCTGGG GCTCTATAGT TCCTACCAGG AAGTGGGGAA 360
TTCCCAGCAG CTTGCAGTGG GTGGTGGGGA GGTGGAGAGG GAGAAGTTTC CAGAGGGTCA 420
GGGCTTCCTT AGGAAGGGCC CTCCCATCCT GAGGCAAATC TCTGCTCATC CCCTGAAGGT 480
AGAAGTGGGC TTTGGGATCC AAGGTGCCCT TTAGCTTGGG ATGTAGGGCA TGTAATTCTT 540
ACTCAAAGGA CAGCCTCTCT CCTCAGGCCT CGGCAAGGAG CCAAGACAGA CGCCCTCTCC 600
TCCAGCAGCC GGCTCCTTGG GGCTCCTCCT CCTCCTCTCC TCCCAGCGCT CCTCGCTGGA 660
CTTCTTTATT CCCCACATTG TCTTCTCATC TCCCTACTGA AACTAGGAGA AGGTGGAGGG 720
AGGGCCTAGA TTGTTCCTCT CTGAAAGGGT CCCCCAGTTG GGTAAGAAGA GCTGGTCTGT 780
GGTCACGGCC TACAATCCAG TAAGCTCGGG CTCTGCCTGT GGCCAAGTTA CTCAGCTACT 840
CCAAGTCCAG GCTTGCTCCT CTGTAAAATG GGGATGCCCC TTTGCAAAGC TGTTGTGCTG 900
AGCCATTGCA TGTCAGACTC CTTGCGAATT CGCTTTAGAG ATTGTTGTTC ATTAGTCGAA 960
CATCCATTCA GCACATTTAT TGTGTGCTCA GTGTGTGCTA TGTGCTGTTC TGTGGGCTGT 1020
TCTGTGGGCT AAGAATGTAG AGTGAACAAA GCAGACAAAA CCCCTGTCCT CCTGGAGCTC 1080
ACACTTTAGT GGGGAAGATG AACAAGAAGG AAGCCAGCAA 1120
|
